A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1113088



Internal ID18907626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:23814558..23814616hg38UCSC Ensembl
Outerchr1:24141048..24141106hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3967981
SamplesKWS2
Known GenesHMGCL
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1113088
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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